» Articles » PMID: 30306076

Diagnostic Insights into Chronic-inflammatory Demyelinating Polyneuropathies

Overview
Journal Ann Transl Med
Date 2018 Oct 12
PMID 30306076
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare immune-mediated neuropathy with demyelination of nerve fibers as leading morphological feature. The course of disease can be chronic progressive or remitting relapsing. Whereas for acute immune-mediated neuropathies several serological markers have been identified and used successfully in clinical routine, the serological diagnosis of chronic variants such as CIDP has not yet been evolved satisfactory. The typical CIDP and its various atypical variants are characterized by a certain diversity of clinical phenotype and response to treatment. Thus, diagnostic markers could aid in the differential diagnosis of CIDP variants and stratification of patients for a better treatment response. Most patients respond well to a causal therapy including steroids, intravenous immunoglobulins and plasmapheresis. Apart from electrophysiological and morphological markers, several autoantibodies have been reported as candidate markers for CIDP, including antibodies against glycolipids or paranodal/nodal molecules. The present review provides a summary of the progress in autoantibody testing in CIDP and its possible implication on the stratification of the CIDP variants and treatment response.

Citing Articles

Chronic Inflammatory Demyelinating Polyneuropathy: A Narrative Review of a Systematic Diagnostic Approach to Avoid Misdiagnosis.

Roman-Guzman R, Martinez-Mayorga A, Guzman-Martinez L, Rodriguez-Leyva I Cureus. 2025; 17(1):e76749.

PMID: 39897200 PMC: 11785518. DOI: 10.7759/cureus.76749.


Molecular, Electrophysiological, and Ultrasonographic Differences in Selected Immune-Mediated Neuropathies with Therapeutic Implications.

Dziadkowiak E, Nowakowska-Kotas M, Ralowska-Gmoch W, Budrewicz S, Koszewicz M Int J Mol Sci. 2023; 24(11).

PMID: 37298132 PMC: 10252615. DOI: 10.3390/ijms24119180.


Principles of Therapeutic Apheresis in Neurological Disease.

Strasser E Transfus Med Hemother. 2023; 50(2):88-97.

PMID: 37066058 PMC: 10091019. DOI: 10.1159/000529463.


Is Fecal Calprotectin an Applicable Biomarker of Gut Immune System Activation in Chronic Inflammatory Demyelinating Polyneuropathy? - A Pilot Study.

Koszewicz M, Mulak A, Dziadkowiak E, Budrewicz S Front Hum Neurosci. 2021; 15:733070.

PMID: 34867240 PMC: 8636096. DOI: 10.3389/fnhum.2021.733070.


Monocentric study of 28 cases of chronic inflammatory demyelinating polyneuropathy: first Tunisian study.

Mansour M, Rachdi A, Baradai N, Kacem A, Bedoui I, Mrissa R Neurol Sci. 2021; 43(1):565-571.

PMID: 33945035 DOI: 10.1007/s10072-021-05153-x.


References
1.
Querol L, Devaux J, Rojas-Garcia R, Illa I . Autoantibodies in chronic inflammatory neuropathies: diagnostic and therapeutic implications. Nat Rev Neurol. 2017; 13(9):533-547. DOI: 10.1038/nrneurol.2017.84. View

2.
Attarian S, Boucraut J, Hubert A, Uzenot D, Delmont E, Verschueren A . Chronic ataxic neuropathies associated with anti-GD1b IgM antibodies: response to IVIg therapy. J Neurol Neurosurg Psychiatry. 2009; 81(1):61-4. DOI: 10.1136/jnnp.2009.185736. View

3.
Burnor E, Yang L, Zhou H, Patterson K, Quinn C, Reilly M . Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies. Neurology. 2017; 90(1):e31-e38. PMC: 5754648. DOI: 10.1212/WNL.0000000000004773. View

4.
Giannotta C, Di Pietro D, Gallia F, Nobile-Orazio E . Anti-sulfatide IgM antibodies in peripheral neuropathy: to test or not to test?. Eur J Neurol. 2015; 22(5):879-82. DOI: 10.1111/ene.12658. View

5.
Pang S, Chan K, Mak W, Kung M, Lee C, Tsoi T . Single-nucleotide polymorphism of transient axonal glycoprotein-1 and its correlation with clinical features and prognosis in chronic inflammatory demyelinating polyneuropathy. J Peripher Nerv Syst. 2012; 17(1):72-5. DOI: 10.1111/j.1529-8027.2012.00380.x. View